US3313641A - Dispersions and process therefor - Google Patents
Dispersions and process therefor Download PDFInfo
- Publication number
- US3313641A US3313641A US324203A US32420363A US3313641A US 3313641 A US3313641 A US 3313641A US 324203 A US324203 A US 324203A US 32420363 A US32420363 A US 32420363A US 3313641 A US3313641 A US 3313641A
- Authority
- US
- United States
- Prior art keywords
- dialdehyde
- dispersions
- polysaccharide
- water
- slurry
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B31/00—Preparation of derivatives of starch
- C08B31/18—Oxidised starch
- C08B31/185—Derivatives of oxidised starch, e.g. crosslinked oxidised starch
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B31/00—Preparation of derivatives of starch
- C08B31/18—Oxidised starch
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
Definitions
- This invention relates to a process for producing a stable dispersion of dialdehyde polysaccharides in water. More particularly, it relates to the process of reacting hydrogen peroxides with a water slurry of dialdehyde polysaccharides and to the novel stable dispersions prepared thereby.
- Dialdehyde polysaccharides such as dialdehyde corn starch
- dialdehyde corn starch are well known in the art and are known to be useful for increasing the wet strength of paper, for example.
- the water solubility and water dispersibility of dialdehyde polysaccharides are quite low and complicated procedures are necessary in order to get adequate dialdehyde polysaccharide into dispersion so that the paper or paper pulp can be treated with it. This is especially true when the dispersions are to be prepared in high concentrations containing as much as 2030 weight percent solids.
- Prior art dispersions of dialdehyde polysaccharides were limited in utility since they became unstable as the polymer chain began to degrade when stored a week or longer at room temperature.
- a dialdehyde polysaccharide-water slurry containing up to about 30 weight percent dialdehyde polysaccharide and substantially free of metal ions is reacted with from about 0.5 to 2.0 weight percent hydrogen peroxide (based on weight of dialdehyde polysaccharide) at a reaction temperature of from about 75 C. to about 95 C.
- the hydrogen peroxide is employed in amounts from about 1 to about 2 weight percent, based on weight of dialdehyde polysaccharide.
- the reaction is continued for a period of from about 30 to 60 minutes and then the resulting dispersion is cooled to room temperature.
- This stable dispersion containing from about 10 to about 30 weight percent dialdehyde polysaccharide can be used immediately or it can be stored at room temperature for several months without change in appearance, viscosity or loss in efiectiveness as a wet strength agent for paper.
- the hydrogen peroxide oxidizes some of the aldehyde groups of the dialdehyde polysaccharide to carboxy groups. This improves thedispersibility.
- the dispersion thus contains a carboxylated dialdehydepolysaccharide.
- dialdehyde polysaccharides useful as starting materials in the present process of preparing stable dispersions are frequently referred so as periodate oxidized polysaccharides. This is due to their preparation by the wellknown oxidation of polysaccharides with periodic acid. This preparation can 'be illustrated by the conversion of starch to dialdehyde starch or periodate oxodized starch using periodic acid in accordance with the following equation:
- dialdehyde polysaccharides useful in preparing dispersions of the present invention may be the dialdehyde derivative of any polysaccharide, such as corn, wheat, rice, tapioca or potato starches, amyloses, amylopectins, celluloses, gums, dextrans, algins, inulins and the like.
- any polysaccharide such as corn, wheat, rice, tapioca or potato starches, amyloses, amylopectins, celluloses, gums, dextrans, algins, inulins and the like.
- dialdehyde derivatives known generically as dialdehyde starch are the best known and most widely used. However, where it is desired to have dispersions of dialdehyde derivatives of other polysaccharides, these may be used as well.
- dialdehyde polysaccharides useful in the present invention can contain from about 0.5 to about 100 mole percent dialdehyde saccharide units. In general, it is preferred to use dialdehyde polysaccharides which are about 90 percent to 100 percent oxidized; i.e., those wherein about 90 to 100 of each 100 of the original anhydroglucose units have been converted to dialdehyde units such as by periodate oxidation as above described.
- the water used in the preparation of the stable dis persions of the present invention should be substantially free of metal ions. Such ions can cause hydrolysis and degradation of the dialdehyde polysaccharides. Distilled water or deionized water can be used in the present invention.
- the hydrogen peroxide useful in the present invention is used in the form of commercially available aqueous solutions containing, for example, from about 30 to about weight percent hydrogen peroxide.
- the overall temperature range useful in the preparation of stable water dispersions of dialdehyde polysaccharides is from about C. to about C. Within this range, the particular temperature is generally dependent upon the dialdehyde polysaccharide concentration in the slurry and the concentration of the hydrogen peroxide supplied for oxidation of some of the aldehyde groups of the dialdehyde poiysaccharide. Higher temperatures are required as the dialdehyde polysaccharide concentration in the slurry increases. There is thus a substantially direct relationship between dialdehyde polysaccharide concentration and reaction temperature. On the other hand, the temperature required tends to decrease as the hydrogen peroxide concentration increases. There is thus a substantially inverse relationship between hydrogen peroxide concentration and reaction temperature.
- the dialdehyde polysaccharide in the presence of hydrogen peroxide, reaches a stage of maximum swelling of the dialdehyde polysaccharide granules at 7595 C. Within about 5-15 minutes. With moderate stirring at this temperature a gradual rupture of the swollen granules occurs and homogeneous dispersions are formed within a period of from about 30 to about 60 minutes of total heating time, depending on temperature, concentration of dialdehyde polysaccharide and total amount hydrogen peroxide used.
- novel dispersions of the present invention comprise the reaction product of a substantially metal ionfree water slurry of dialdehyde polysaccharide and hydrogen peroxide wherein such reaction was carried out at about 75-95 C. for about 30-60 minutes.
- These dispersions are quite stable and can be used in a well-known known manner employing 21 Noble and Wood Handsheet Machine. These sheets were dried for 2 minutes at 200 F. (933 (3.). Similar handsheets were prepared from the same paper pulp slurry but which had not been treated manner to impart wet strength improvements to paper. 5 with the cationic dispersion.
- novel dispersions of the present invention are handsheets were soaked in room temperature d1st1lled used for paper treatment they are preferably used in water for 5 minutes and the tensile strengths were meascombination with a cationizing agent or retention aid ured by standard techniques.
- the handsheets prepared to assist in coupling the dialdehyde polysaccharide to the from pulp that had been treated with the novel dialdehyde paper fibers.
- These cationizing agents or retention aids polysaccharide dispersion of the present invention had an are the well-known cationic starches, polymeric amines average wet tensile strength of 7.4 lbs/1n. of Width. and polyamides.
- the cationizing agent can be added first Paper prepared from untreated pulp had average wet to a slurry of paper pulp followed by addition of the tensile strength of only 1.6 lbs./in. of width. After a dialdehyde polysaccharide dispersion or the cationizing storage time of 3 months, an aliquot part of the Example agent and the dialdehyde polysaccharide dispersion can be 1 dispersion was eaiiOIliZed With Zirconium oxyehlofide mixed together and this mixture applied to the paper and added to paper pulp in the same manner as described pulp lurry, Water soluble compounds of ir onium, above using same concentrations of dispersion, cationsuch as Zirconium oxychloride, can also be used as cationizing agent and pulp.
- Handsheets prepared from this izing agents. treated pulp had average wet tensile strength of 7.0 lbs./
- the following examples serve to illustrate, but not to in. of width. This clearly shows the improved stability limit, the practice of th inve tio over prolonged storage periods of the novel dispersions
- Example 1 of the present invention prepared by a novel process. To an open beaker, equipped with stirrer and ther- Example 3 mometer, and placed in a steam bath, were charged 500 2; Various dlspersions of dialdehyde polysaccharides in m1. of distilled water and 150 g.
- dialdehyde polysaccharide peramre f three months During this storage period used as raw material was the same as described in Exthere were no signs of instability, polymer degradation or ample For companson Purposes, the e tenslle viscosity change strengths were measured for handsheets employing as the Example 2 wet strength agents prior art dispersions of dialdehyde polysaccharides in water.
- a process for preparing stable dispersions of dialdehyde polysaccharides in Water which comprises forming a slurry of dialdehyde polysaccharide in substantially metal ion-free water, said slurry containing up to about 30 Weight percent solids, contacting said slurry with from about 0.5 to about 2.0 weight percent hydrogen peroxide based on weight of dialdehyde polysaccharide, said contact taking place at a reaction temperature of from about 75 C. to about 95 C. for a period of from about 30 to about 60 minutes, and then cooling the resulting dispersion to room temperature.
- a process for preparing stable dispersions of dialdehyde polysaccharides in water which comprises forming a slurry of dialdehyde polysaccharide in substantially metal ion-free Water, said slurry containing from about to about 30 Weight percent solids, contacting said slurry with from about 1 to about 2 Weight percent hydrogen peroxide based on Weight of dialdehyde polysaccharide, said contact taking place at a reaction temperature of from about 75 C. to about 95 C. for a period of from about 30 to about 60 minutes, and then cooling the resulting dispersion to room temperature.
- dialdehyde polysaccharide contains from about 0.5 to about 100 mole percent dialdehyde saccharide units.
- dialdehyde polysaccharide contains from about 90 to about 100 mole percent dialdehyde saccharide units.
- dialdehyde polysaccharide contains from about 0.5 to about 100 mole percent dialdehyde saccharide units.
- dialdehyde polysaccharide contains from about 90 to about 100 mole percent dialdehyde saccharide units.
- a stable dispersion of carboxylated dialdehyde polysaccharide in Water which comprises the room temperature cooled product resulting from the reaction of a substantially metal ion-free water slurry of dialdehyde polysaccharide containing up to Weight percent solids with from about 0.5 to about 2.0 weight percent hydrogen peroxide based on weight of dialdehyde polysaccharide, wherein such reaction was carried out at about 95 C. for about 30-60 minutes.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Paper (AREA)
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1054386D GB1054386A (ru) | 1963-11-18 | ||
US324203A US3313641A (en) | 1963-11-18 | 1963-11-18 | Dispersions and process therefor |
FR995281A FR1425344A (fr) | 1963-11-18 | 1964-11-17 | Procédé de fabrication de dispersion stable de dialdéhyde-polysaccharides |
BE655854D BE655854A (ru) | 1963-11-18 | 1964-11-17 | |
SE13855/64A SE312544B (ru) | 1963-11-18 | 1964-11-17 | |
DEM63175A DE1241433B (de) | 1963-11-18 | 1964-11-18 | Verfahren zur Herstellung von stabilen waessrigen Dispersionen von teilweise oxydierten Dialdehydpolysacchariden |
CH1490064A CH438003A (de) | 1963-11-18 | 1964-11-18 | Stabile Dialdehyd-Polysaccharid-Dispersionen und Verfahren zu ihrer Herstellung |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US324203A US3313641A (en) | 1963-11-18 | 1963-11-18 | Dispersions and process therefor |
Publications (1)
Publication Number | Publication Date |
---|---|
US3313641A true US3313641A (en) | 1967-04-11 |
Family
ID=23262554
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US324203A Expired - Lifetime US3313641A (en) | 1963-11-18 | 1963-11-18 | Dispersions and process therefor |
Country Status (6)
Country | Link |
---|---|
US (1) | US3313641A (ru) |
BE (1) | BE655854A (ru) |
CH (1) | CH438003A (ru) |
DE (1) | DE1241433B (ru) |
GB (1) | GB1054386A (ru) |
SE (1) | SE312544B (ru) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3479427A (en) * | 1965-10-22 | 1969-11-18 | Dart Ind Inc | Composition for application to hair |
US3540905A (en) * | 1968-01-22 | 1970-11-17 | Miles Lab | Process for stable dispersions of dialdehyde polysaccharides |
US4041233A (en) * | 1976-03-15 | 1977-08-09 | Nasa | Aldehyde-containing urea-absorbing polysaccharides |
US6409881B1 (en) | 1999-11-08 | 2002-06-25 | Sca Hygiene Products Gmbh | Metal-crosslinkable oxidized cellulose-containing fibrous materials and products made therefrom |
US6635755B1 (en) | 1999-11-08 | 2003-10-21 | Sca Hygiene Products Gmbh | Oxidized polymeric carbohydrates and products made thereof |
US6824645B2 (en) | 1999-02-24 | 2004-11-30 | Sca Hygiene Products Gmbh | Oxidized cellulose-containing fibrous materials and products made therefrom |
US20060263510A1 (en) * | 2005-05-18 | 2006-11-23 | Roman Skuratowicz | Hydroxyl radical modification of carbohydrates |
US8507666B2 (en) | 2010-08-24 | 2013-08-13 | Corn Products Development, Inc. | Modification of carbohydrates using continuous generation of hydroxyl radicals |
US9512563B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Surface treated modified cellulose from chemical kraft fiber and methods of making and using same |
US9512561B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
US9512237B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Method for inhibiting the growth of microbes with a modified cellulose fiber |
US9511167B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
US9951470B2 (en) | 2013-03-15 | 2018-04-24 | Gp Cellulose Gmbh | Low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same |
CN109053913A (zh) * | 2018-07-03 | 2018-12-21 | 青岛农业大学 | 采用离子凝胶法制备淀粉纳米颗粒的方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2669523A (en) * | 1952-08-28 | 1954-02-16 | Corn Produets Refining Company | Cold water dispersible starch sizes and process of making them |
US2894945A (en) * | 1956-12-19 | 1959-07-14 | Bernard T Hofreiter | Dicarboxyl starches and method of preparation |
US3081199A (en) * | 1959-10-06 | 1963-03-12 | Staley Mfg Co A E | Modified starch product for coating cellulosic webs |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3033851A (en) * | 1961-04-18 | 1962-05-08 | Wilbur C Schaefer | Heterofunctional derivatives of dialdehyde starches and method of making same |
-
0
- GB GB1054386D patent/GB1054386A/en active Active
-
1963
- 1963-11-18 US US324203A patent/US3313641A/en not_active Expired - Lifetime
-
1964
- 1964-11-17 BE BE655854D patent/BE655854A/xx unknown
- 1964-11-17 SE SE13855/64A patent/SE312544B/xx unknown
- 1964-11-18 DE DEM63175A patent/DE1241433B/de active Pending
- 1964-11-18 CH CH1490064A patent/CH438003A/de unknown
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2669523A (en) * | 1952-08-28 | 1954-02-16 | Corn Produets Refining Company | Cold water dispersible starch sizes and process of making them |
US2894945A (en) * | 1956-12-19 | 1959-07-14 | Bernard T Hofreiter | Dicarboxyl starches and method of preparation |
US3081199A (en) * | 1959-10-06 | 1963-03-12 | Staley Mfg Co A E | Modified starch product for coating cellulosic webs |
Cited By (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3479427A (en) * | 1965-10-22 | 1969-11-18 | Dart Ind Inc | Composition for application to hair |
US3540905A (en) * | 1968-01-22 | 1970-11-17 | Miles Lab | Process for stable dispersions of dialdehyde polysaccharides |
US4041233A (en) * | 1976-03-15 | 1977-08-09 | Nasa | Aldehyde-containing urea-absorbing polysaccharides |
US6824645B2 (en) | 1999-02-24 | 2004-11-30 | Sca Hygiene Products Gmbh | Oxidized cellulose-containing fibrous materials and products made therefrom |
US6409881B1 (en) | 1999-11-08 | 2002-06-25 | Sca Hygiene Products Gmbh | Metal-crosslinkable oxidized cellulose-containing fibrous materials and products made therefrom |
US6635755B1 (en) | 1999-11-08 | 2003-10-21 | Sca Hygiene Products Gmbh | Oxidized polymeric carbohydrates and products made thereof |
US20040010137A1 (en) * | 1999-11-08 | 2004-01-15 | Sca Hygiene Products Gmbh | Oxidized polymeric carbohydrates and products made thereof |
US6987181B2 (en) | 1999-11-08 | 2006-01-17 | Sca Hygiene Products Gmbh | Oxidized polymeric carbohydrates and products made thereof |
US20060263510A1 (en) * | 2005-05-18 | 2006-11-23 | Roman Skuratowicz | Hydroxyl radical modification of carbohydrates |
US9512562B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
US10106927B2 (en) | 2009-05-28 | 2018-10-23 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
US9512561B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
USRE49570E1 (en) | 2009-05-28 | 2023-07-04 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
US9512237B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Method for inhibiting the growth of microbes with a modified cellulose fiber |
US9511167B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
US9777432B2 (en) | 2009-05-28 | 2017-10-03 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
US9909257B2 (en) | 2009-05-28 | 2018-03-06 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
US11111628B2 (en) | 2009-05-28 | 2021-09-07 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
US9512563B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Surface treated modified cellulose from chemical kraft fiber and methods of making and using same |
US10731293B2 (en) | 2009-05-28 | 2020-08-04 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
US8507666B2 (en) | 2010-08-24 | 2013-08-13 | Corn Products Development, Inc. | Modification of carbohydrates using continuous generation of hydroxyl radicals |
US10174455B2 (en) | 2013-03-15 | 2019-01-08 | Gp Cellulose Gmbh | Low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same |
US10294614B2 (en) | 2013-03-15 | 2019-05-21 | Gp Cellulose Gmbh | Low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same |
US10550516B2 (en) | 2013-03-15 | 2020-02-04 | Gp Cellulose Gmbh | Low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same |
US10753043B2 (en) | 2013-03-15 | 2020-08-25 | Gp Cellulose Gmbh | Low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same |
US9951470B2 (en) | 2013-03-15 | 2018-04-24 | Gp Cellulose Gmbh | Low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same |
CN109053913A (zh) * | 2018-07-03 | 2018-12-21 | 青岛农业大学 | 采用离子凝胶法制备淀粉纳米颗粒的方法 |
Also Published As
Publication number | Publication date |
---|---|
BE655854A (ru) | 1965-05-17 |
GB1054386A (ru) | |
CH438003A (de) | 1967-06-15 |
DE1241433B (de) | 1967-06-01 |
SE312544B (ru) | 1969-07-21 |
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